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Mendeleev Communications, 2019, Volume 29, Issue 2, Pages 153–154
DOI: https://doi.org/10.1016/j.mencom.2019.03.011
(Mi mendc1453)
 

This article is cited in 13 scientific papers (total in 13 papers)

Communications

Phosphorylation of (1-aryl-1-hydroxymethyl)phosphonates

Z. Radaia, V. Hodulaa, N. Z. Kissa, J. Kotib, G. T. Keglevicha

a Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest, Hungary
b Spectroscopic Research Division, Gedeon Richter Plc., Budapest, Hungary
Abstract: The reaction of dimethyl (1-aryl-1-hydroxymethyl)phosphonates with 1-chloro-3-phospholene 1-oxides, diphenylphosphinic chloride or diphenyl chloridophosphonate affords the corresponding (1-phosphoryloxymethyl)phosphonates. The products with two different >P(O)– moieties exhibit characteristic δP shifts and 3JP,P couplings in the 31P NMR spectra.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (571.7 Kb)


Citation: Z. Radai, V. Hodula, N. Z. Kiss, J. Koti, G. T. Keglevich, “Phosphorylation of (1-aryl-1-hydroxymethyl)phosphonates”, Mendeleev Commun., 29:2 (2019), 153–154
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  • This publication is cited in the following 13 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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